Fortrea

The Associate Director/Director PO & P2P Management is a senior leadership role accountable for the endtoend P2P lifecycle from requisition and purchase order creation support invoice processing and supplier payment. This role drives process excellence compliance automation and cost

The Associate Director/Director PO & P2P Management is a senior leadership role accountable for the endtoend P2P lifecycle from requisition and purchase order creation support invoice processing and supplier payment. This role drives process excellence compliance automation and cost

Our FSP team is currently seeking an Oncology Sr. CRA 2 with 5 years of monitoring residing in the NYC Metro. WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to provide a high standard of care for participants in clinical trials and respond to emergency s

Our FSP team is currently seeking an Oncology Sr. CRA 2 with 5 years of monitoring residing in the NYC Metro. WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to provide a high standard of care for participants in clinical trials and respond to emergency s

We are seeking a highly skilled Workday PSA (Professional Services Automation) Architect to join our dynamic IT team. The ideal candidate will have extensive experience in Workday PSA and how to successfully deliver the solution within the challenges of the matrix environment. As a Wo

We are seeking a highly skilled Workday PSA (Professional Services Automation) Architect to join our dynamic IT team. The ideal candidate will have extensive experience in Workday PSA and how to successfully deliver the solution within the challenges of the matrix environment. As a Wo

The Site Budget & Contracts Specialist is responsible for drafting negotiating and managing site agreements and related clinical trial contracts for Sponsor-led studies. The role ensures timely execution of agreements compliance with SOPs and ICH-GCP principles and close collaboration

The Site Budget & Contracts Specialist is responsible for drafting negotiating and managing site agreements and related clinical trial contracts for Sponsor-led studies. The role ensures timely execution of agreements compliance with SOPs and ICH-GCP principles and close collaboration

As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in the UK and US. We are currently seeking a Screening Technician to interact directly with our healthy volunteer participants while learning to read clinical research p

As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in the UK and US. We are currently seeking a Screening Technician to interact directly with our healthy volunteer participants while learning to read clinical research p

As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in the UK and US.We are seeking an Operations Coordinator to provide administrative and logistical support for clinical research this role you will partner closely with

As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in the UK and US.We are seeking an Operations Coordinator to provide administrative and logistical support for clinical research this role you will partner closely with

Our FSP team is currently seeking an Oncology Sr. CRA 2 with 5 years of monitoring residing in the Los Angeles or Southern California. WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to provide a high standard of care for participants in clinical trials a

Our FSP team is currently seeking an Oncology Sr. CRA 2 with 5 years of monitoring residing in the Los Angeles or Southern California. WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to provide a high standard of care for participants in clinical trials a

Join one of the worlds largest Clinical Research Organizations and support early-phase clinical trials in a fastpaced highly collaborative environment. As a Clinical Research Coordinator you will oversee the operational execution of assigned studies ensuring compliance with protocols

Join one of the worlds largest Clinical Research Organizations and support early-phase clinical trials in a fastpaced highly collaborative environment. As a Clinical Research Coordinator you will oversee the operational execution of assigned studies ensuring compliance with protocols

As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in the UK and US.We are currently seeking an Outpatient Visit (OPV) Research Nurse to lead and support our Clinical Pharmacology Start-up team in initiating Early Phase

As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in the UK and US.We are currently seeking an Outpatient Visit (OPV) Research Nurse to lead and support our Clinical Pharmacology Start-up team in initiating Early Phase

Our FSP team is currently seeking an Oncology Sr. CRA 2 with 5 years of monitoring residing in the Midwest (Louisville Cincinnati or Indianapolis). WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to provide a high standard of care for participants in clin

Our FSP team is currently seeking an Oncology Sr. CRA 2 with 5 years of monitoring residing in the Midwest (Louisville Cincinnati or Indianapolis). WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to provide a high standard of care for participants in clin

Our FSP department in Spain is looking for a CRA II to work for one of our sponsor and managing clinical studies in Oncology Hematology and Immunology . Full remote role you need to be based in Galicia preferably in Santiago de Compostela and La Coruña.Main Responsibilities: Clinical

Our FSP department in Spain is looking for a CRA II to work for one of our sponsor and managing clinical studies in Oncology Hematology and Immunology . Full remote role you need to be based in Galicia preferably in Santiago de Compostela and La Coruña.Main Responsibilities: Clinical

Job Overview:Site monitoring and site management responsibility for clinical studies according to Company and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. Assures the implementation of project plans as assigned.Summary of Responsibilities:Responsible for all asp

Job Overview:Site monitoring and site management responsibility for clinical studies according to Company and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. Assures the implementation of project plans as assigned.Summary of Responsibilities:Responsible for all asp

Summary of Responsibilities:Site management responsibility for clinical studies according to Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and Sponsor requirements including verification of study training records.Conducts site monitoring responsibi

Summary of Responsibilities:Site management responsibility for clinical studies according to Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and Sponsor requirements including verification of study training records.Conducts site monitoring responsibi

The RCM Billing Manager will be responsible for all processes and resources related to billing procedures including project / contract setup invoicing processing rebates and processing credits and rebills but not limited to the following:Summary of Responsibilities: Effectively manage

The RCM Billing Manager will be responsible for all processes and resources related to billing procedures including project / contract setup invoicing processing rebates and processing credits and rebills but not limited to the following:Summary of Responsibilities: Effectively manage

Fortrea is growing! For one of our client we are currently looking for a Start-Up Specialist.Responsibilities (but not only):Serve as primary contact for investigative sites and ensure documents required are collected in a timely manner.May support the negotiation of site contracts an

Fortrea is growing! For one of our client we are currently looking for a Start-Up Specialist.Responsibilities (but not only):Serve as primary contact for investigative sites and ensure documents required are collected in a timely manner.May support the negotiation of site contracts an

Job Overview:Provides support to the Regional Manager of Compensation including data collection salary surveys job evaluation and report preparation. Assists in global processes such as compensation review cycles and ensures accuracy confidentiality and compliance in compensation-rela

Job Overview:Provides support to the Regional Manager of Compensation including data collection salary surveys job evaluation and report preparation. Assists in global processes such as compensation review cycles and ensures accuracy confidentiality and compliance in compensation-rela

Job Overview: The Head of Global Procurement Service Center reports directly to the Chief Procurement Officer and is responsible for matrix managing the local Bangalore resources that report to procurement leaders that are not local to Bangalore. This team consists of individuals that

Job Overview: The Head of Global Procurement Service Center reports directly to the Chief Procurement Officer and is responsible for matrix managing the local Bangalore resources that report to procurement leaders that are not local to Bangalore. This team consists of individuals that

Job Overview:The Platform Reliability & Observability Lead (SRE) will own and elevate the reliability availability and operational excellence of its hosting and platform services. This is an engineering led role accountable for measurable reliability outcomes across cloud and hybrid e

Job Overview:The Platform Reliability & Observability Lead (SRE) will own and elevate the reliability availability and operational excellence of its hosting and platform services. This is an engineering led role accountable for measurable reliability outcomes across cloud and hybrid e

Fortrea is looking for an experienced Clinical Trial Assistant to support global clinical studies within an FSP model for a leading pharmaceutical sponsor.What youll do:Support clinical trials endtoend in close collaboration with Clinical Project Managers and CROsManage study document

Fortrea is looking for an experienced Clinical Trial Assistant to support global clinical studies within an FSP model for a leading pharmaceutical sponsor.What youll do:Support clinical trials endtoend in close collaboration with Clinical Project Managers and CROsManage study document

Main ResponsibilitiesThe Central Monitoring Specialist is responsible for the execution of key Central Monitoring (Site subject & study level review as applicable) activities and in assisting the execution of several key activities.The Central Monitoring Specialist collaborates with t

Main ResponsibilitiesThe Central Monitoring Specialist is responsible for the execution of key Central Monitoring (Site subject & study level review as applicable) activities and in assisting the execution of several key activities.The Central Monitoring Specialist collaborates with t